The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
125227301 12522730 1 I 20160612 20160630 20160701 20160701 EXP CO-ABBVIE-16P-036-1666344-00 ABBVIE 19.33 YR F Y 54.00000 KG 20160701 CN COUNTRY NOT SPECIFIED CO

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
125227301 12522730 1 PS ZEMPLAR PARICALCITOL 1 Intravenous (not otherwise specified) Y UNKNOWN 20819 5 UG INJECTION
125227301 12522730 2 C OMEPRAZOLE. OMEPRAZOLE 1 0
125227301 12522730 3 C CLONIDINE. CLONIDINE 1 0
125227301 12522730 4 C PREDNISOLONE. PREDNISOLONE 1 0
125227301 12522730 5 C NYSTATIN. NYSTATIN 1 0
125227301 12522730 6 C TACROLIMUS. TACROLIMUS 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125227301 12522730 1 Hyperparathyroidism secondary
125227301 12522730 2 Product used for unknown indication
125227301 12522730 3 Product used for unknown indication
125227301 12522730 4 Product used for unknown indication
125227301 12522730 5 Product used for unknown indication
125227301 12522730 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125227301 12522730 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125227301 12522730 Renal transplant

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
125227301 12522730 1 20151028 20160610 0